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RPL7AP28 ribosomal protein L7a pseudogene 28 [ Homo sapiens (human) ]

Gene ID: 100271209, updated on 17-Sep-2024

Summary

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Official Symbol
RPL7AP28provided by HGNC
Official Full Name
ribosomal protein L7a pseudogene 28provided by HGNC
Primary source
HGNC:HGNC:35656
See related
Ensembl:ENSG00000184139 AllianceGenome:HGNC:35656
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
RPL7A_10_519
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Genomic context

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See RPL7AP28 in Genome Data Viewer
Location:
4q28.3
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 4 NC_000004.12 (131857340..131857907, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 4 NC_060928.1 (135181141..135181708, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 4 NC_000004.11 (132778495..132779062, complement)

Chromosome 4 - NC_000004.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC124900859 Neighboring gene uncharacterized LOC124900177 Neighboring gene uncharacterized LOC105377425 Neighboring gene small nucleolar RNA host gene 27 Neighboring gene uncharacterized LOC105377428 Neighboring gene ReSE screen-validated silencer GRCh37_chr4:133042782-133042957 Neighboring gene NANOG-H3K4me1 hESC enhancer GRCh37_chr4:133045368-133046113 Neighboring gene NANOG-H3K4me1 hESC enhancer GRCh37_chr4:133046114-133046858 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr4:133090465-133090966 Neighboring gene elongation factor for RNA polymerase II 2 pseudogene 2

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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Related articles in PubMed

  1. Comparative analysis of processed ribosomal protein pseudogenes in four mammalian genomes. Balasubramanian S, et al. Genome Biol, 2009. PMID 19123937, Free PMC Article

GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

General gene information

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NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

Genomic

  1. NG_010540.1 

    Range
    101..668
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000004.12 Reference GRCh38.p14 Primary Assembly

    Range
    131857340..131857907 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060928.1 Alternate T2T-CHM13v2.0

    Range
    135181141..135181708 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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